• Thumbnail for Renpenning's syndrome
    Renpenning's syndrome is a neurodevelopmental disorder recognised in males that causes intellectual disability, mild growth retardation with examples...
    3 KB (339 words) - 08:38, 18 August 2023
  • Thumbnail for Fragile X syndrome
    Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder characterized by mild-to-moderate intellectual disability. The average IQ in males with...
    59 KB (6,781 words) - 13:44, 7 October 2024
  • Thumbnail for Narrow face
    delay-hypotonia syndrome Renpenning syndrome Seckel syndrome 9 Severe X-linked myotubular myopathy SIN3A-related intellectual disability syndrome due to a point...
    4 KB (224 words) - 07:14, 15 April 2024
  • deletion syndrome 22q11.2 duplication syndrome 22q13 deletion syndrome 2p15-16.1 microdeletion syndrome 2q37 deletion syndrome 3-M syndrome 3C syndrome 3q29...
    42 KB (4,070 words) - 17:09, 1 October 2024
  • Thumbnail for PQBP1
    in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly"...
    28 KB (3,107 words) - 00:17, 13 August 2024
  • Thumbnail for Micrognathism
    Prolidase deficiency Pyknodysostosis RAB23-related Carpenter syndrome Renpenning syndrome Restrictive dermopathy 1 RFT1-congenital disorder of glycosylation...
    14 KB (1,343 words) - 13:07, 21 September 2024
  • Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. Syndromic...
    13 KB (538 words) - 09:46, 18 March 2024
  • dysgenesis; 267430; REN Renal-hepatic-pancreatic dysplasia; 208540; NPHP3 Renpenning syndrome; 309500; PQBP1 Restrictive dermopathy, lethal; 275210; ZMPSTE24 Reticular...
    234 KB (18,877 words) - 15:43, 9 May 2024